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Placenta Accreta: Harrowing Stories Emerge

Summary

  • PAS often goes undiagnosed, increasing severe bleeding risk.
  • Women faced emergency surgery and PTSD from PAS.
  • Campaigners highlight systemic failures in maternity care.
Placenta Accreta: Harrowing Stories Emerge

A campaign to raise awareness of placenta accreta spectrum (PAS) has brought to light the devastating experiences of numerous women in the UK and abroad. Since its February launch, scores of women have recounted how medical staff failed to detect this rare but potentially fatal pregnancy complication, leading to emergency surgeries and significant health consequences.

PAS occurs when the placenta grows too deeply into the uterus, complicating separation after birth. Women have suffered catastrophic blood loss, requiring hysterectomies and blood transfusions. One former operating theatre nurse now suffers from PTSD and has changed careers due to her PAS experience. Another woman blames her daughter's cerebral palsy on a stroke suffered during a traumatic birth complicated by undiagnosed PAS.

Campaigners, including Amisha and Nik Adhia of Action for Accreta, have collated 100 cases, with 61% of these women reporting their PAS went undiagnosed. They highlight "dangerous gaps in maternity care" and "systemic failures" within the NHS, calling for improved staff training and a more robust system for identifying and managing PAS. Politicians are supporting calls for a major overhaul.

Factors increasing PAS risk include a history of C-section births and assisted fertility treatments like IVF. Several women, such as Erin Cooper and Chloe Robinson, shared their critical experiences, including massive hemorrhages and life-saving hysterectomies. These accounts underscore the urgent need for better diagnostic infrastructure and clinical preparedness across UK hospitals.

Disclaimer: This story has been auto-aggregated and auto-summarised by a computer program. This story has not been edited or created by the Feedzop team.

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